510(k) Report

510(k) · Cleared

Cleared

Primatrix Dermal Repair Scaffold

K083440510(k) SpecialCleared Dec 12, 200822-day reviewClass U

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Tei Biosciences, Inc. · KGN Wound Dressing With Animal-Derived Material (S)

Cleared on Dec 12, 2008 as substantially equivalent to K061407 (Tei Biosciences, Inc., 2006) and 1 other predicate after a 22-day review. Its family tree reaches back 5 generations to 1988. 20 later devices descend from it.

Decided
Dec 12, 2008
Review
22 days
Class
Class U
Product code
KGN
Recalls
None
Predicates
2

Its longest line of descent runs back 5 generations to K881854 (1988). 11 ancestors in all. 20 later devices descend from it, 4 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2006: 1 other ancestor1998: 1 other ancestor1993: 1 other ancestor1991: 3 other ancestors2010: 1 descendant cleared2012: 2 descendants cleared2013: 2 descendants cleared2017: 2 descendants cleared2016: 3 descendants cleared2019: 1 descendant cleared2014: 1 descendant cleared2025: 3 descendants cleared2021: 1 descendant cleared2022: 1 descendant cleared2024: 1 descendant cleared2018: 1 descendant cleared2026: 1 descendant clearedK881854 · Sorbsan Topical Wound Dressing · E.G. Dick & Assoc. · 1988K982597 · Fibrcol Plus Collagen Wound Dressing with Alginate · Johnson & Johnson Medical, Inc. · 1998K993948 · Sis Wound Dressing II · Cook Biotech, Inc. · 2000K023778 · Dressskin · Tei Biosciences, Inc. · 2003K061407 · Primatrix Dermal Repair Scaffold · Tei Biosciences, Inc. · 20061990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 1 other ancestor4 generations back: 5 other ancestors 1 generation forward: 4 descendants2 generations forward: 5 descendants3 generations forward: 7 descendants4 generations forward: 4 descendants K061407 · Primatrix Dermal Repair Scaffold · Tei Biosciences, Inc. · 2006K023778 · Dressskin · Tei Biosciences, Inc. · 2003K993948 · Sis Wound Dressing II · Cook Biotech, Inc. · 2000K982597 · Fibrcol Plus Collagen Wound Dressing with Alginate · Johnson & Johnson Medical, Inc. · 1998K881854 · Sorbsan Topical Wound Dressing · E.G. Dick & Assoc. · 1988−50
  1. Root · 5 generations backK881854 Sorbsan Topical Wound DressingE.G. Dick & Assoc. · 1988
  2. 4 generations backK982597 Fibrcol Plus Collagen Wound Dressing with AlginateJohnson & Johnson Medical, Inc. · 1998
  3. 3 generations backK993948 Sis Wound Dressing IICook Biotech, Inc. · 2000
  4. 2 generations backK023778 DressskinTei Biosciences, Inc. · 2003
  5. 1 generation backK061407 Primatrix Dermal Repair ScaffoldTei Biosciences, Inc. · 2006
  6. This deviceK083440 Primatrix Dermal Repair ScaffoldTei Biosciences, Inc. · 2008
  7. Descendant · cites it directly · 6 of its ownK100261 Primatrix AG Antimicrobial Dermal Dermal Repair ScaffoldTei Biosciences, Inc. · 2010 · Recalled
  8. Descendant · cites it directly · 5 of its ownK132343 Marigen Wound DressingKerecis Limited · 2013
  9. Descendant · cites it directly · 5 of its ownK131286 Primatrix Dermal Repair ScaffoldTei Biosciences, Inc. · 2013
  10. Descendant · 2 generations on · 4 of its ownK153690 PriMatrix Dermal Repair ScaffoldTei Biosciences, Inc. · 2016 · Recalled
  11. Descendant · 2 generations on · 4 of its ownK120605 Permacol Surgical ImplantCovidien, LLC · 2012

Showing 5 of 20 descendants. See all descendants

Descendants cleared per year

2010: 12012: 22013: 22014: 12016: 32017: 22018: 12019: 12021: 12022: 12024: 12025: 32026: 1
2010high 3 (2016) · low 0 (2011)2026

Most influential descendants

Showing 5 of 20 · See all
  • K100261Primatrix AG Antimicrobial Dermal Dermal Repair ScaffoldTei Biosciences, Inc. · 2010 · cites it directly6descendants
  • K132343Marigen Wound DressingKerecis Limited · 2013 · cites it directly5descendants
  • K131286Primatrix Dermal Repair ScaffoldTei Biosciences, Inc. · 2013 · cites it directly5descendants
  • K153690PriMatrix Dermal Repair ScaffoldTei Biosciences, Inc. · 2016 · 2 generations on4descendants
  • K120605Permacol Surgical ImplantCovidien, LLC · 2012 · 2 generations on4descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K881854Sorbsan Topical Wound DressingE.G. Dick & Assoc.1988—
−4K982597Fibrcol Plus Collagen Wound Dressing with AlginateJohnson & Johnson Medical, Inc.1998—
−3K993948Sis Wound Dressing IICook Biotech, Inc.2000—
−2K023778DressskinTei Biosciences, Inc.2003—
−1K061407Primatrix Dermal Repair ScaffoldTei Biosciences, Inc.2006—
0 (this device)K083440Primatrix Dermal Repair ScaffoldTei Biosciences, Inc.2008—
+1K100261Primatrix AG Antimicrobial Dermal Dermal Repair ScaffoldTei Biosciences, Inc.20103
+1K132343Marigen Wound DressingKerecis Limited2013—
+1K131286Primatrix Dermal Repair ScaffoldTei Biosciences, Inc.2013—
+2K153690PriMatrix Dermal Repair ScaffoldTei Biosciences, Inc.20164
+2K120605Permacol Surgical ImplantCovidien, LLC2012—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199130
199310
199810
200610

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201010
201220
201320
201410
201630
201720
201810
201910
202110
202210
202410
202530
202610
FIG. 1 — Lineage of K083440, 1988–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in KGN? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new KGN device

  1. #1 K231325 Corplex P / Theracor P / Allacor Pscore 17.9 · 8 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (2)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K061407Primatrix Dermal Repair Scaffold
Summary page 1
…on and intended use to: Predicate Devices Manufacturer 510(k) Number PriMatrix TE! Biosciences K061407 Oasis Cook Biotech K061711 -15- === Pag…
Tei Biosciences, Inc.2006—
*K061711Oasis Wound Matrix
Summary page 1
…rer 510(k) Number PriMatrix TE! Biosciences K061407 Oasis Cook Biotech K061711 -15- TEl BIOSCIENCES INC. PriMatrix Derm…
Cook Biotech, Inc.2006—

Also cleared against K061407: 1 other device →

What descends from it? (20)

See all 20

4 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K100261Primatrix AG Antimicrobial Dermal Dermal Repair ScaffoldTei Biosciences, Inc.20106
K132343Marigen Wound DressingKerecis Limited20135
K131286Primatrix Dermal Repair ScaffoldTei Biosciences, Inc.20135
K113866Porcine Dermal Xenografts Porcine Dermal MatrixBrennen Medical, LLC20120

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 20 years and passes through 4 companies; a new generation was cleared every 2.7 years on median.
  • None of the 11 ancestors has a recall.
  • Of its descendants, K100261 (Tei Biosciences, Inc., 2010) has gone furthest, with 6 descendants of its own.
  • 1 other device also cites its predicate K061407.

How does its category compare?

All KGN devices

KGN Wound Dressing With Animal-Derived Material (S): FDA decisions, review times, recalls and adverse event reports over 20 years. 2008, this device’s year, is highlighted.

FDA decisions per year · KGN

15so far in 2026, the most since 2007

2007: 32008: 62009: 82010: 42011: 72012: 82013: 62014: 52015: 72016: 42017: 72018: 62019: 32020: 52021: 62022: 122023: 92024: 132025: 102026 (partial year): 15
2007high 15 (2026) · low 3 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KGN

162in 2025

2007: 32 days median2008: 87 days median2009: 121 days median2010: 175 days median2011: 228 days median2012: 123 days median2013: 147 days median2014: 188 days median2015: 87 days median2016: 164 days median2017: 136 days median2018: 148 days median2019: 128 days median2020: 279 days median2021: 236 days median2022: 246 days median2023: 194 days median2024: 83 days median2025: 162 days median2026 (partial year): 174 days median
2007high 279 (2020) · low 32 (2007)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · KGN

3in 2018

2017: 12018: 3
2007high 3 (2018) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · KGN

15in 2025

2008: 12009: 22010: 32011: 62012: 42013: 62014: 122015: 92016: 62017: 82018: 152019: 112020: 172021: 142022: 132023: 212024: 152025: 15
2007high 21 (2023) · low 0 (2007)2025

MAUDE reports naming product code KGN, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
200733200
200868701
2009812102
2010417503
2011722806
2012812304
2013614706
20145188012
201578709
2016416406
2017713618
20186148315
20193128011
20205279017
20216236014
202212246013
20239194021
20241383015
202510162015
2026151740—

What is it indicated for?

PriMatrix is intended for the management of wounds that include:

* Partial and full thickness wounds

* Pressure, diabetic, and venous ulcers

· Second-degree burns

• Surgical wounds-donor sites/grafts, post-Mohs surgery, post-laser surgery, podiatric, wound dehiscence

· Trauma wounds-abrasions, lacerations, and skin tears

· Tunneled/undermined wounds

· Draining wounds

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K083440: Primatrix Dermal Repair Scaffold.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K083440

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026